FDA Inspection 749662 — ActiTech, LP

ActiTech, LP — FEI 3007005869

The FDA completed an inspection of ActiTech, LP on August 23, 2011 in Sherman, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 23, 2011
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Sherman, TX (United States)